Matsumoto T, Miake S, Mitsuyama M, Takeya K, Nomoto K
Department of Microbiology, School of Medicine, Kyushu University, Fukuoka, Japan.
J Clin Lab Immunol. 1979 Apr;2(1):55-8.
Protective mechanisms against Listeria monocytogenes were studied in young (3-month-old) and old (15-month-old) mice of C3H/He strain. Cumulative mortality rates of old mice were lower than those of young mice after intravenous inoculation of the same doses of bacteria. The numbers of bacteria in the liver and spleen on days 1 and 3 were larger in young than old mice. Bacterial growth at this stage of infection is suppressed by accumulation of non-immune macrophages. On day 7, however, the numbers of bacteria in the liver were smaller in young than old mice. Bacterial elimination at this stage depends upon immune macrophages. These results suggest that the enhanced resistance to lethal effects of bacteria in old mice may be ascribed to activation of non-immune macrophages in the presence of depressed capacities to raise cell-mediated immunity.
在C3H/He品系的年轻(3个月大)和年老(15个月大)小鼠中研究了针对单核细胞增生李斯特菌的保护机制。静脉注射相同剂量细菌后,老年小鼠的累积死亡率低于年轻小鼠。在第1天和第3天,年轻小鼠肝脏和脾脏中的细菌数量比老年小鼠多。在感染的这个阶段,非免疫巨噬细胞的积累会抑制细菌生长。然而,在第7天,年轻小鼠肝脏中的细菌数量比老年小鼠少。在这个阶段细菌的清除取决于免疫巨噬细胞。这些结果表明,老年小鼠对细菌致死作用的抵抗力增强可能归因于在细胞介导免疫能力下降的情况下非免疫巨噬细胞的激活。